Bert Ba de Vries

564 total citations
7 papers, 305 citations indexed

About

Bert Ba de Vries is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Bert Ba de Vries has authored 7 papers receiving a total of 305 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Cognitive Neuroscience. Recurrent topics in Bert Ba de Vries's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Bert Ba de Vries is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Bert Ba de Vries collaborates with scholars based in Netherlands, Australia and Canada. Bert Ba de Vries's co-authors include Martinus F. Niermeijer, Ben A. Oostra, D. J. J. Halley, Eveline Wesby–van Swaay, J. O. Van Hemel, J. P. Fryns, Merlin G. Butler, David A. Koolen, Simone Mandelstam and Kenneth A. Myers and has published in prestigious journals such as Epilepsia, Journal of Medical Genetics and Europe PMC (PubMed Central).

In The Last Decade

Bert Ba de Vries

6 papers receiving 293 citations

Peers

Bert Ba de Vries

GENET

MB

CN

CP

CMN

Teresa Lim United States

Maria Pintaudi Italy

Bàrbara Torrico Spain

J.A.S. Vorstman Netherlands

Tamika Malone United States

Joana Almeida Portugal

Wei‐Hsien Chien Taiwan

Monica B. Proud United States

Amy Lawson‐Yuen United States

Jasmine Paquin Canada

Teresa Lim United States

Bert Ba de Vries

215 ×0.8

GENET

127 ×0.8

MB

161 ×1.3

CN

18 ×0.9

CP

21 ×1.2

CMN

Citations per year, relative to Bert Ba de Vries Bert Ba de Vries (= 1×) peers Teresa Lim

Countries citing papers authored by Bert Ba de Vries

Since Specialization

Citations

This map shows the geographic impact of Bert Ba de Vries's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Bert Ba de Vries with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bert Ba de Vries more than expected).

Fields of papers citing papers by Bert Ba de Vries

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bert Ba de Vries. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Bert Ba de Vries. The network helps show where Bert Ba de Vries may publish in the future.

Co-authorship network of co-authors of Bert Ba de Vries

This figure shows the co-authorship network connecting the top 25 collaborators of Bert Ba de Vries. A scholar is included among the top collaborators of Bert Ba de Vries based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bert Ba de Vries. Bert Ba de Vries is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

1.

Myers, Kenneth A., Simone Mandelstam, Georgia Ramantani, et al.. (2017). The epileptology of Koolen‐de Vries syndrome: Electro‐clinico‐radiologic findings in 31 patients. Epilepsia. 58(6). 1085–1094. 20 indexed citations

2.

Varvagiannis, Konstantinos, Bert Ba de Vries, & Lisenka E.L.M. Vissers. (2017). WAC-Related Intellectual Disability. Europe PMC (PubMed Central). 1 indexed citations

3.

Bon, Bregje W.M. van, Heather C. Mefford, & Bert Ba de Vries. (2015). 15q13.3 Microdeletion. Europe PMC (PubMed Central).

4.

Koolen, David A. & Bert Ba de Vries. (2013). KANSL1-Related Intellectual Disability Syndrome. 6 indexed citations

5.

Vries, Bert Ba de, D. J. J. Halley, Ben A. Oostra, & Martinus F. Niermeijer. (1998). The fragile X syndrome.. Journal of Medical Genetics. 35(7). 579–589. 190 indexed citations

6.

Vries, Bert Ba de, et al.. (1997). DNA testing for fragile X syndrome: implications for parents and family.. Journal of Medical Genetics. 34(11). 907–911. 15 indexed citations

7.

Vries, Bert Ba de, J. P. Fryns, Merlin G. Butler, et al.. (1993). Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.. Journal of Medical Genetics. 30(9). 761–766. 73 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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